Evidence map›Paper›PMID 23122959›Full record

ArticleCell reports2012

Normal spastin gene dosage is specifically required for axon regeneration.

Michelle C Stone, Kavitha Rao, Kyle W Gheres, Seahee Kim, Juan Tao, Caroline La Rochelle, Christin T Folker, Nina T Sherwood, Melissa M Rolls

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
1.5field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. SPG4 Hereditary Spastic Paraplegia: From Etiology to Therapy.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
  3. Article
  4. Article
  5. eNeuro · 2026
    Article
  6. Peripheral Nerve Crush inCold Spring Harbor protocols · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. The Role of Spastin in Axon Biology.Frontiers in cell and developmental biology · 2022
    Review
  15. Article
  16. Therapeutic Strategies for MutantBrain sciences · 2021
    Review
  17. Review
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Michelle C StoneDepartment of Biochemistry and Molecular Biology, Penn State, University Park, PA 16802, USA.
Kavitha Rao
Kyle W Gheres
Seahee Kim
Juan Tao
Caroline La Rochelle
Christin T Folker
Nina T Sherwood
Melissa M Rolls
Pennsylvania State University · USDuke University · US

Funding

Using Drosophila Neurons to Identify Mechanisms that Control Microtubule PolarityR01GM085115 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Melissa Rolls · 2010 to 2026
$5.1M
Genetic Analysis of the Roles and Regulation of Microtubule Severing in NeuronsR01NS063896 · NINDS · DUKE UNIVERSITY · PI SHERWOOD, NINA TANG · 2008 to 2011
$1.0M
Neuronal events and molecular pathways in active dendrite degenerationR21NS066216 · NINDS · PENNSYLVANIA STATE UNIVERSITY, THE · PI ROLLS, MELISSA · 2009 to 2010
$355k
NIGMS NIH HHS R01 GM085115NINDS NIH HHS R01 NS063896NINDS NIH HHS R01 NS63896NINDS NIH HHS R21 NS066216
6 · The paper itself

Abstract

Axon regeneration allows neurons to repair circuits after trauma; however, most of the molecular players in this process remain to be identified. Given that microtubule rearrangements have been observed in injured neurons, we tested whether microtubule-severing proteins might play a role in axon regeneration. We found that axon regeneration is extremely sensitive to levels of the microtubule-severing protein spastin. Although microtubule behavior in uninjured neurons was not perturbed in animals heterozygous for a spastin null allele, axon regeneration was severely disrupted in this background. Two types of axon regeneration-regeneration of an axon from a dendrite after proximal axotomy and regeneration of an axon from the stump after distal axotomy-were defective in Drosophila with one mutant copy of the spastin gene. Other types of axon and dendrite outgrowth, including regrowth of dendrites after pruning, were normal in heterozygotes. We conclude that regenerative axon growth is uniquely sensitive to spastin gene dosage.

Indexed as

Adenosine TriphosphatasesAllelesAnimalsAxonsDendritesDrosophilaDrosophila ProteinsGene DosageKataninMicrotubulesMutationNerve RegenerationRNA InterferenceRNA, Small InterferingTubulinAdenosine TriphosphatasesDrosophila ProteinsKat-60L1 protein, DrosophilaKataninRNA, Small Interferingspas protein, DrosophilaTubulin

Identifiers

PMID23122959
PMCPMC3513560
OpenAlexW2001221488

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.